Bleeding Thrombotic and Platelet Disorder TIER1 genes (v.ISTH_2019.1) Gene Category Associated disorder(s) Inheritance Transcript Location symbol Bleeding/coagulation F10 Factor X deficiency AR; AD NM_000504.3 13q34 Bleeding/coagulation F11 Factor XI deficiency AR; AD NM_000128.3 4q35.2 Coagulation Factor XII deficiency AR (coagulation) F12 NM_000505.3 5q35.3 Angioedema Angioedema AD (angioedema) Bleeding/coagulation F13A1 Factor XIII deficiency AR NM_000129.3 6p25.1 Bleeding/coagulation F13B Factor XIII deficiency AR NM_001994.2 1q31.3 Bleeding/coagulation ProthroMbin deficiency AR (bleeding/coagulation) Thrombosis F2 Thrombophilia due to AD (thrombosis) NM_000506.4 11p11.2 thrombin defect Bleeding/coagulation Factor V deficiency AR (bleeding/coagulation) Thrombosis F5 Thrombophilia due to AD (thrombosis) NM_000130.4 1q24.2 activated protein C resistance Bleeding/coagulation F7 Factor VII deficiency AR; AD NM_000131.4 13q34 Bleeding/coagulation F8 HaeMophilia A XLR NM_000132.3 Xq28 Bleeding/coagulation F9 HaeMophilia B XLR NM_000133.3 Xq27.1 AR (afibrinogeneMia); Bleeding FGA Fibrinogen deficiency AD NM_000508.3 4q31.3 (hypo/dysfibrinogeneMia) AR (afibrinogeneMia); Bleeding FGB Fibrinogen deficiency AD NM_005141.4 4q31.3 (hypo/dysfibrinogeneMia) AR (afibrinogeneMia); Bleeding FGG Fibrinogen deficiency AD NM_021870.2 4q32.1 (hypo/dysfibrinogeneMia) VitaMin K-dependent clotting Bleeding/coagulation GGCX AR NM_000821.6 2p11.2 factors deficiency 1 Coagulation KNG1 Kininogen Deficiency AR NM_000893.4 3q27.3 CoMbined factor V and VIII Bleeding/coagulation LMAN1 AR NM_005570.3 18q21.32 deficiency CoMbined factor V and VIII NM_139279.5 Bleeding/coagulation MCFD2 AR 2p21 deficiency PlasMinogen activator Bleeding SERPINE1 AR; AD NM_000602.4 7q22.1 Inhibitor 1 deficiency Bleeding SERPINF2 Alpha 2 antiplasMin deficiency AR NM_000934.3 17p13.3 VitaMin K-dependent clotting Bleeding/coagulation VKORC1 AR NM_024006.5 16p11.2 factors deficiency 2 Bleeding AD (VWD type 1 and 2) VWF Von Willebrand disease AR (VWD type 3) NM_000552.3 12p13.31 Platelet AD (VWD type 2B) ThroMbotic ThroMbosis ADAMTS13 throMbocytopenic purpura AR NM_139025.4 9q34.2 (TTP) Histidine-rich glycoprotein ThroMbosis HRG AD NM_000412.4 3q27.3 deficiency ParoxysMal nocturnal ThroMbosis PIGA acquired (somatic) NM_002641.3 Xp22.2 heMoglobinuria ThroMbosis PLG PlasMinogen deficiency AR NM_000301.3 3q27.3 ThroMbosis PROC Protein C deficiency AR; AD NM_000312.3 Xp22.2 Bleeding Thrombotic and Platelet Disorder TIER1 genes (v.ISTH_2019.1) ThroMbosis PROS1 Protein S deficiency AR; AD NM_000313.3 3q27.3 ThroMbosis SERPINC1 AntithroMbin deficiency AR; AD NM_000488.3 1q25.1 ThroMbosis SERPIND1 Heparin cofactor 2 deficiency AD NM_000185.3 22q11.21 ThroMbosis ThroMboModulin deficiency; THBD Bleeding due to high soluble AD NM_000361.2 20p11.21 Bleeding thrombomodulin SitosteroleMia with Platelet ABCG5 AR NM_022436.2 2p21 macrothrombocytopenia SitosteroleMia with Platelet ABCG8 AR NM_022437.2 2p21 macrothrombocytopenia Baraitser-Winter syndroMe 1 Platelet ACTB AD NM_001101.3 7p22.1 with macrothroMbocytopenia Platelet ACTN1 MacrothroMbocytopenia AD NM_001130004.1 14q24.1 Platelet ANKRD26 AD throMbocytopenia 2 AD NM_014915.2 10p12.1 Platelet ANO6 Scott syndroMe AR NM_001025356.2 12q12 Platelet AP3B1 HerMansky-Pudlak syndroMe AR NM_003664.4 5q14.1 Platelet AP3D1 HerMansky-Pudlak syndroMe AR NM_001261826.3 19p13.3 Platelet abnorMalities with eosinophilia and iMMune- Platelet ARPC1B AR NM_005720.4 7q22.1 mediated inflammatory disease Platelet BLOC1S3 HerMansky-Pudlak syndroMe AR NM_212550.4 19q13.32 Platelet BLOC1S6 HerMansky-Pudlak syndroMe AR NM_012388.3 15q21.1 Takenouchi-Kosaki syndroMe Platelet CDC42 AD NM_001791.4 1p36.12 with throMbocytopenia Platelet CYCS AD throMbocytopenia 4 AD NM_018947.5 7p15.3 MacrothroMbocytopenia and Platelet DIAPH1 AD NM_001079812.2 5q31.3 sensorineural hearing loss Platelet DTNBP1 HerMansky-Pudlak syndroMe AR NM_032122.4 6p22.3 ThroMbocytopenia and Platelet ETV6 AD NM_001987.4 12p13.2 susceptibility to cancer Leukocyte integrin adhesion Platelet FERMT3 AR NM_178443.2 11q13.1 deficiency, type 3 Paris-Trousseau and Jacobson NM_002017.4 Platelet FLI1 AR; AD 11q24.3 syndroMe SyndroMe with Platelet FLNA XLD; XLR NM_001110556.2 Xq28 macrothrombocytopenia Platelet FYB1 ThroMbocytopenia 3 AR NM_001465.6 5p13.1 X-linked throMbocytopenia Platelet GATA1 XR NM_002049.3 Xp11.23 with dyserythropoiesis Platelet-type bleeding Platelet GFI1B AD; AR NM_004188.5 9q34.13 disorder 17 Platelet GNE Myopathy associated with TP AR NM_005476.6 9p13.3 Bernard-Soulier syndroMe AR (BSS) Mild MacrothroMbocytopenia AD (Mild MacroTP) Platelet GP1BA NM_000173.5 17p13.2 Platelet-type von Willebrand AD (platelet-type von disease Willebrand) Bernard-Soulier syndroMe AR (BSS) Platelet GP1BB NM_000407.4 22q11.21 Mild macrothroMbocytopenia AD (Mild MacroTP) Bleeding diathesis due to Platelet GP6 AR NM_016363.5 19q13.42 glycoprotein VI deficiency Bleeding Thrombotic and Platelet Disorder TIER1 genes (v.ISTH_2019.1) Platelet GP9 Bernard-Soulier syndroMe AR NM_000174.4 3q21.3 Amegakaryocytic Platelet HOXA11 throMbocytopenia with AD NM_005523.5 7p15.2 radioulnar synostosis Platelet HPS1 HerMansky-Pudlak syndroMe AR NM_000195.4 10q24.2 Platelet HPS3 HerMansky-Pudlak syndroMe AR NM_032383.4 3q24 Platelet HPS4 HerMansky-Pudlak syndroMe AR NM_022081.5 22q12.1 Platelet HPS5 HerMansky-Pudlak syndroMe AR NM_181507.1 11p15.1 Platelet HPS6 HerMansky-Pudlak syndroMe AR NM_024747.5 10q24.32 Platelet IKZF5 ThroMbocytopenia AD n/a 10q26.13 GlanzMann throMbasthenia AR (GT) Platelet ITGA2B Platelet-type bleeding AD (bleeding disorder) NM_000419.3 17q21.31 disorder 16 GlanzMann throMbasthenia AR (GT) Platelet ITGB3 Platelet-type bleeding AD (bleeding disorder) NM_000212.2 17q21.32 disorder 16 ThroMbocytopenia and Platelet KDSR AR NM_002035.4 18q21.33 erythrokeraderMa Platelet LYST Chediak-Higashi syndroMe AR NM_000081.3 1q42.3 Amegakaryocytic Platelet MECOM throMbocytopenia with AD NM_004991.3 3q26.2 radioulnar synostosis 2 ThroMbocytopenia, anaeMia Platelet MPIG6B AR NM_025260.3 6p21.33 and Myelofibrosis Congenital aMegakaryocytic Platelet MPL AR NM_005373.2 1p34.2 throMbocytopenia Platelet MYH9 MYH9-related disorders AD NM_002473.5 22q12.3 AutisM with platelet dense Platelet NBEA AD NM_015678.4 13q13.3 granule defect Platelet NBEAL2 Gray platelet syndroMe AR NM_015175.2 3p21.31 Platelet P2RY12 ADP receptor defect AR NM_022788.4 3q25.1 Deficiency of phospholipase Platelet PLA2G4A AR NM_024420.2 1q31.1 A2, group IV A Platelet PLAU Quebec platelet disorder AD NM_002658.3 10q22.2 Platelet-type bleeding Platelet RASGRP2 AR NM_153819.1 11q13.1 disorder 18 Platelet RBM8A TP-absent radius syndrome AR NM_005105.4 1q21.1 Platelet RNU4ATAC RoifMan SyndroMe AR NR_023343.1 2q14.2 FaMilial platelet disorder with Platelet RUNX1 AD NM_001754.4 21q22.12 predisposition to AML Platelet-type bleeding Platelet SLFN14 AD NM_001129820.1 17q12 disorder 20 Platelet SRC ThroMbocytopenia 6 AD NM_198291.2 20q11.23 StorMorken syndroMe (York Platelet STIM1 AD NM_003156.3 11p15.4 platelet syndroMe) FaMilial heMophagocytic Platelet STXBP2 AR NM_006949.2 19p13.2 lyMphohistiocytosis type 5 ThroMboxane A2 receptor Platelet TBXA2R AR; AD (partial phenotype) NM_001060.5 19p13.3 defect Platelet TBXAS1 Ghosal syndroMe AR NM_030984.3 7q34 Bleeding Thrombotic and Platelet Disorder TIER1 genes (v.ISTH_2019.1) ThroMbocytopenia Platelet THPO progressing to trilineage bone AR NM_000460.4 3q27.1 marrow failure Platelet TUBB1 MacrothroMbocytopenia AD NM_030773.3 20q13.32 Arthrogryposis, renal Platelet VIPAS39 AR NM_001193315.1 14q24.3 dysfunction, and cholestasis 1 Arthrogryposis, renal Platelet VPS33B AR NM_018668.4 15q26.1 dysfunction, and cholestasis 2 Platelet WAS Wiskott-Aldrich syndroMe XLR NM_000377.2 Xp11.23 AD: autosoMal doMinant. AR: autosoMal recessive. XLD: X-linked doMinant. XLR: X-linked recessive. Categories in italics indicate a rarer occurrence for a specific gene. .